510(k) K060836
K060836 is an FDA 510(k) premarket notification submitted by Dentsply Intl., Inc. for the device "VISTADENT OC - VERSION 4". The FDA issued a decision of Substantially Equivalent on October 27, 2006. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Dentsply Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 2006
- Date Received
- March 28, 2006
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type